Immunogenicity of the RTS,S/AS01 malaria vaccine and implications for duration of vaccine efficacy: secondary analysis of data from a phase 3 randomised controlled trial

被引:243
作者
White, Michael T. [1 ]
Verity, Robert [1 ]
Griffin, Jamie T. [1 ]
Asante, Kwaku Poku [2 ]
Owusu-Agyei, Seth [2 ,3 ]
Greenwood, Brian [3 ]
Drakeley, Chris [3 ]
Gesase, Samwel [4 ]
Lusingu, John [4 ,5 ]
Ansong, Daniel [6 ]
Adjei, Samuel [7 ]
Agbenyega, Tsiri [6 ]
Ogutu, Bernhards [8 ]
Otieno, Lucas [8 ]
Otieno, Walter [8 ]
Agnandji, Selidji T. [9 ,10 ,11 ]
Lell, Bertrand [9 ,10 ,11 ]
Kremsner, Peter [9 ,10 ,11 ]
Hoffman, Irving [12 ]
Martinson, Francis [13 ]
Kamthunzu, Portia [13 ]
Tinto, Halidou [14 ]
Valea, Innocent [14 ]
Sorgho, Hermann [14 ]
Oneko, Martina [15 ]
Otieno, Kephas [15 ]
Hamel, Mary J. [16 ]
Salim, Nahya [17 ]
Mtoro, Ali [17 ]
Abdulla, Salim [17 ]
Aide, Pedro [18 ]
Sacarlal, Jahit [18 ,19 ]
Aponte, John J. [18 ,20 ]
Njuguna, Patricia [21 ]
Marsh, Kevin [22 ,23 ]
Bejon, Philip [21 ,22 ]
Riley, Eleanor M. [3 ]
Ghani, Azra C. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, MRC Ctr Outbreak Anal & Modelling, Dept Infect Dis Epidemiol, London W2 1PG, England
[2] Kintampo Hlth Res Ctr, Kintampo, Ghana
[3] Univ London London Sch Hyg & Trop Med, London, England
[4] Tanzania Natl Inst Med Res, Dar Es Salaam, Tanzania
[5] Univ Copenhagen, Copenhagen, Denmark
[6] Kwame Nkrumah Univ Sci & Technol, Sch Med Sci, Kumasi, Ghana
[7] Agogo Presbyterian Hosp, Agogo, Ghana
[8] KEMRI Walter Reed Project, Kombewa, Kenya
[9] Ctr Rech Med Lambarene, Lambarene, Gabon
[10] Univ Klinikum Tubingen, Inst Tropenmed, Tubingen, Germany
[11] German Ctr Infect Res, Tubingen, Germany
[12] Univ N Carolina, Dept Med, Chapel Hill, NC USA
[13] Univ North Carolina Project Malawi, Lilongwe, Malawi
[14] Inst Natl Rech Sci Sante, Nanoro, Burkina Faso
[15] KEMRI CDC Publ Hlth & Res Collaborat, Kisumu, Kenya
[16] US Ctr Dis Control & Prevent, Malaria Branch, Div Parasit Dis & Malaria, Atlanta, GA USA
[17] Bagamoyo Res & Training Ctr, Ifakara Hlth Inst, Bagamoyo, Tanzania
[18] Ctr Invest Saude Manhica, Manhica, Mozambique
[19] Univ Eduardo Mondlane, Fac Med, Maputo, Mozambique
[20] Hosp Clin Univ Barcelona, ISGlobal, Barcelona Ctr Int Hlth Res, Barcelona, Spain
[21] KEMRI Wellcome Trust Res Programme, Kilifi, Kenya
[22] Univ Oxford, Nuffield Dept Med, Oxford, England
[23] African Acad Sci, Nairobi, Kenya
基金
英国医学研究理事会;
关键词
PLASMODIUM-FALCIPARUM INFECTION; PROTECTION; ANTIBODY; IMMUNIZATION; MECHANISMS; IMMUNITY; DISEASE; BLIND;
D O I
10.1016/S1473-3099(15)00239-X
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background The RTS,S/AS01 malaria vaccine targets the circumsporozoite protein, inducing antibodies associated with the prevention of Plasmodium falciparum infection. We assessed the association between anti-circumsporozoite antibody titres and the magnitude and duration of vaccine efficacy using data from a phase 3 trial done between 2009 and 2014. Methods Using data from 8922 African children aged 5-17 months and 6537 African infants aged 6-12 weeks at first vaccination, we analysed the determinants of immunogenicity after RTS,S/AS01 vaccination with or without a booster dose. We assessed the association between the incidence of clinical malaria and anti-circumsporozoite antibody titres using a model of anti-circumsporozoite antibody dynamics and the natural acquisition of protective immunity over time. Findings RTS,S/AS01-induced anti-circumsporozoite antibody titres were greater in children aged 5-17 months than in those aged 6-12 weeks. Pre-vaccination anti-circumsporozoite titres were associated with lower immunogenicity in children aged 6-12 weeks and higher immunogenicity in those aged 5-17 months. The immunogenicity of the booster dose was strongly associated with immunogenicity after primary vaccination. Anti-circumsporozoite titres wane according to a biphasic exponential distribution. In participants aged 5-17 months, the half-life of the short-lived component of the antibody response was 45 days (95% credible interval 42-48) and that of the long-lived component was 591 days (557-632). After primary vaccination 12% (11-13) of the response was estimated to be long-lived, rising to 30% (28-32%) after a booster dose. An anti-circumsporozoite antibody titre of 121 EU/mL (98-153) was estimated to prevent 50% of infections. Waning anti-circumsporozoite antibody titres predict the duration of efficacy against clinical malaria across different age categories and transmission intensities, and efficacy wanes more rapidly at higher transmission intensity. Interpretation Anti-circumsporozoite antibody titres are a surrogate of protection for the magnitude and duration of RTS,S/AS01 efficacy, with or without a booster dose, providing a valuable surrogate of effectiveness for new RTS,S formulations in the age groups considered.
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收藏
页码:1450 / 1458
页数:9
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